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Completed Phase 4 Interventional

A Study Measuring Asthma Control In Pediatric And Adolescent Subjects Whose Asthma Is Worsened By Activity Or Exercise

ClinicalTrials.gov ID: NCT00118690

Public ClinicalTrials.gov record NCT00118690. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 5:38 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Stratified, Multicenter, Randomized, Double-Blind, Parallel Group, 4-Week Comparison of Fluticasone Propionate/Salmeterol DISKUS Combination Product 100/50mcg BID Versus Fluticasone Propionate DISKUS 100mcg BID in Pediatric and Adolescent Subjects With Activity-Induced Bronchospasm

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

During this study, your child will need to attend up to 5 office visits and maintain regular telephone contact with the clinic. Certain office visits will include physical exams, medical history review, exercise challenge test (walking/running on a treadmill), electrocardiogram (ECG) tests, and lung function tests. All study related medications and medical examinations are provided at no cost. All study drugs are currently available by prescription to patients 4 years and older.

Study identification

NCT ID
NCT00118690
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
227 participants

Conditions and interventions

Eligibility (public fields only)

Age range
4 Years to 17 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2003 (Type not available)
Primary completion
Dec 2005 (Actual)
Completion
Dec 2005 (Actual)
Last update posted
Sep 23, 2016

2003 – 2005

United States locations

U.S. sites
51
U.S. states
25
U.S. cities
48
Facility City State ZIP Site status
GSK Investigational Site Jonesboro Arkansas 72401 —
GSK Investigational Site East Artesia California 90706 —
GSK Investigational Site Huntington Beach California 92647 —
GSK Investigational Site Long Beach California 90806 —
GSK Investigational Site Los Angeles California 90015 —
GSK Investigational Site Madera California 93638 —
GSK Investigational Site Mission Viejo California 92691 —
GSK Investigational Site Oakland California 94618 —
GSK Investigational Site Rolling Hills Est California 90274 —
GSK Investigational Site Vista California 92083 —
GSK Investigational Site Denver Colorado 80206 —
GSK Investigational Site Englewood Colorado 80112 —
GSK Investigational Site Pueblo Colorado 81008 —
GSK Investigational Site Altamonte Springs Florida 32701 —
GSK Investigational Site Delray Beach Florida 33484 —
GSK Investigational Site St. Petersburg Florida 33710 —
GSK Investigational Site Tampa Florida 33607 —
GSK Investigational Site Tampa Florida 33613 —
GSK Investigational Site Lawrenceville Georgia 30045 —
GSK Investigational Site Marietta Georgia 30062 —
GSK Investigational Site Savannah Georgia 31406 —
GSK Investigational Site Savannah Georgia 31419 —
GSK Investigational Site Normal Illinois 61761 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Louisville Kentucky 40202 —
GSK Investigational Site Sunset Louisiana 70584 —
GSK Investigational Site Bethesda Maryland 20814 —
GSK Investigational Site Boston Massachusetts 02111 —
GSK Investigational Site Robbinsdale Minnesota 55422 —
GSK Investigational Site Missoula Montana 59804 —
GSK Investigational Site Omaha Nebraska 68114 —
GSK Investigational Site Mount Laurel New Jersey 08054 —
GSK Investigational Site Kernersville North Carolina 27284 —
GSK Investigational Site Oklahoma City Oklahoma 73120 —
GSK Investigational Site Medford Oregon 97504 —
GSK Investigational Site Altoona Pennsylvania 16601 —
GSK Investigational Site Pittsburgh Pennsylvania 15241 —
GSK Investigational Site Upland Pennsylvania 19013 —
GSK Investigational Site Charleston South Carolina 29407 —
GSK Investigational Site Mt. Pleasant South Carolina 29464 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Nashville Tennessee 37203-1424 —
GSK Investigational Site Dallas Texas 75230 —
GSK Investigational Site El Paso Texas 79902 —
GSK Investigational Site El Paso Texas 79925 —
GSK Investigational Site Houston Texas 77054 —
GSK Investigational Site San Antonio Texas 78205 —
GSK Investigational Site Layton Utah 84041 —
GSK Investigational Site Provo Utah 84604 —
GSK Investigational Site South Burlington Vermont 05403 —
GSK Investigational Site Burke Virginia 22015 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00118690, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 23, 2016 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00118690 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →